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isareverse™+

by Move-Up 3 variants

Ref 0017I1612

isareverse™+ (0017I1612) is a Class III device made by Move-Up, registered in EUDAMED on 12 Jun 2026 (Basic UDI-DI B-03701160201210), active as of 25 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03701160201210 Basic UDI-DI 03701160201210UDI-DIDate12 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
isareverse™+Embase glénoïdienne augmentée 16° Ø 26 mm sans ciment plot longueur 12 mm à vis centrale
Model / reference
0017I1612
Primary DI / UDI-DI
03701160201210
Basic UDI-DI
B-03701160201210
EMDN code
P09010301 Metal back and metaglene glenoid baseplates
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000412

Similar devices in this category

Other devices filed under METAL BACK AND METAGLENE GLENOID BASEPLATES.

Other devices from Move-Up

See all devices from Move-Up →

Properties

  • Supplied sterile
  • Implantable
Other properties (10, all answered No)